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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
15
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pubmed:dateCreated |
1990-9-4
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pubmed:abstractText |
Senescent cell antigen (SCA), an aging antigen, is a protein that appears on old cells and marks them for removal by the immune system in mammals. It is derived from band 3, a ubiquitous membrane transport protein found in diverse cell types and tissues. We have used synthetic peptides to identify aging antigenic sites on band 3, using a competitive inhibition assay and immunoblotting with IgG directed against the aging antigen on old cells. Results indicate that: (i) the active antigenic sites of the aging antigen reside on membrane protein band 3 residues that are extracellular regions implicated in anion transport (residues 538-554 and 788-827); (ii) a putative ankyrin-binding-region peptide is not involved in SCA activity; and (iii) carbohydrate moieties are not required for the antigenicity or recognition of SCA because synthetic peptides alone abolish binding of senescent cell IgG to erythrocytes. One of the putative transport sites that contributes to the aging antigen is located toward the carboxyl terminus. A model of band 3 is presented. Localization of the active antigenic site on the band 3 molecule facilitates definition of the molecular changes occurring during aging that initiate molecular as well as cellular degeneration.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-1059140,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-108480,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-1690071,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-2461589,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-2527366,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-2722777,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-2829189,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3016705,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3087983,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3179456,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3223947,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3377362,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3458208,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3517151,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3521657,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3529979,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-3883494,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-4055737,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-4600883,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-486455,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-492324,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6185837,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6196779,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6207531,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6466875,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6546423,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6572929,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6662217,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6688379,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6830791,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6838541,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-6854266,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-7108955,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-7114050,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-7162219,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-7227479,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1696010-7464917
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5734-8
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:1696010-Amino Acid Sequence,
pubmed-meshheading:1696010-Anion Exchange Protein 1, Erythrocyte,
pubmed-meshheading:1696010-Antigen-Antibody Complex,
pubmed-meshheading:1696010-Antigens, Differentiation,
pubmed-meshheading:1696010-Binding, Competitive,
pubmed-meshheading:1696010-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:1696010-Epitopes,
pubmed-meshheading:1696010-Erythrocyte Aging,
pubmed-meshheading:1696010-Erythrocyte Membrane,
pubmed-meshheading:1696010-Humans,
pubmed-meshheading:1696010-Immunoglobulin G,
pubmed-meshheading:1696010-Models, Molecular,
pubmed-meshheading:1696010-Molecular Sequence Data,
pubmed-meshheading:1696010-Peptides,
pubmed-meshheading:1696010-Protein Conformation
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pubmed:year |
1990
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pubmed:articleTitle |
Definition of a physiologic aging autoantigen by using synthetic peptides of membrane protein band 3: localization of the active antigenic sites.
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pubmed:affiliation |
Department of Medicine, Texas A&M University, Temple 76503.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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